Jenny Kite
Jenny's Story

Jenny joined Watsi on January 26th, 2016. 17 other people also joined Watsi on that day! Jenny's most recent donation traveled 8,200 miles to support Gabriel, a farm worker from Uganda, to treat his broken arm.

Impact

Jenny has funded healthcare for 12 patients in 5 countries.

Patients funded by Jenny

Born in Kenya only one month ago, baby Joy is the second child in her family. Joy’s mother brought her to our medical partner, African Mission Healthcare Foundation (AMHF), seeking treatment for spina bifida. Spina bifida is a birth defect in which several vertebrae in the lower back do not close properly, leaving the baby’s spinal canal exposed. The spinal cord and its surrounding membranes protrude through the opening in the backbone, forming a sac on the baby’s lower back. “Joy has a leaking mass on her lower backbone area,” explains AMHF. Because tissues and nerves in the mass are exposed, “Joy is at a risk of infection” in addition to “development of a tethered [spinal] cord that can lead to either scoliosis or kyphosis and potentially loss of muscle function in her lower limbs.” Without immediate intervention, Joy may also experience urinary and bowel incontinence. Joy’s condition poses significant challenges for her family, as “looking after Joy requires round-the-clock care, from administering her care to ensuring Joy is hygienically clean to avoid infections that may result in fatality,” AMHF tells us. Joy’s mother, a single parent, cares not only for her two children but also for her grandmother who is ill. The money that she earns from washing clothes in the neighborhood is barely enough to support the family, let alone pay for Joy’s medical care. For $805, surgeons will place Joy’s spinal cord and membranes back inside the spinal canal and close the opening on Joy’s back. Funding for Joy also covers the costs of a five-day hospital stay, three days of physical therapy, imaging, lab work, and medicine. “The surgery will help prevent risk of infections, developing tethered cord, and paralysis of Joy’s legs,” says AMHF. “My biggest joy would be to have my little princess treated and successful in future—free from any disability or illness,” shares Joy’s mother.

$805raised
Fully funded

"We would like to ask for help for the treatment of our son. We are greatly concerned for his future," share the parents of 14-month-old Archiel. Archiel lives with his family in the Philippines, and has been diagnosed with unilateral clubfoot. "Archiel cannot walk, he is only capable of rolling from left to right," shares our medical partner, International Care Ministries (ICM). "His mother observed that he has poor locomotive and speech development. This makes it hard for them to address his needs and keep him safe. One parent has to stay in the house and watch him all the time and that prevents his parents to work and sustain their family's needs." "Archiel gives his parents so much joy," ICM continues. "Though he cannot speak or walk, he manages to give happiness to his family by smiling and giggling when he is happy. Those simple moments are greatly cherished by the family. His parents are working together to supply for the needs of the family, but still, their income is not even enough for the needs of the children. That is why it is very hard for them to provide for his treatment." For $1,500, Archiel will receive treatment and surgery to correct his clubfoot. After surgery, "Archiel will be more comfortable in facing challenges in learning and development. As part of him is being treated, this can pave the way that other conditions can also be addressed. This surgery will also increase the quality of life of their family as it address the emotional needs, physical needs, and economic needs that is attached to his condition. With the surgery, he can now also start learning and developing his locomotive skills which will also hasten all other learning stages he has to face in his age," ICM adds. "We have been praying that our time to work for our family will be more than what we can do now," Archiel's parents add, "So the future of our children will be brighter. We also would like our life to become a testimony that God truly touches lives and hearts to help the poor like us. We would like to see Archiel grow, walk, go to school and fulfill whatever dream he has."

$1,500raised
Fully funded

Meet Jeremy, the oldest of three children in his family. Jeremy, a seven-year-old from Kenya, “was born with a mass swelling between his eyes that has continued to grow and worsen with age,” says our medical partner, African Mission Healthcare Foundation (AMHF). Jeremy’s condition, know as a frontal encephalocele, is a defect characterized by a sac-like protrusion of the brain and the membranes that cover it through an opening in the skull. As he grew older, Jeremy began to experience impaired sight, labored breathing, difficulty performing simple tasks, fainting if his swelling was touched, and bullying from his peers. “If not treated, Jeremy may have mental and growth retardation,” says AMHF. His condition has the potential to be life threatening, but Jeremy’s parents have hope that he will receive the surgery he needs to overcome this risk. “Jeremy’s parents are merely casual laborers who struggle to find whatever little work they can," AMHF shares. "With their income being very little, they struggle to put food on the table for their three children.” As a result of their financial situation, Jeremy’s family requires assistance to cover the $780 encephalocele repair surgery that will reduce Jeremy’s chances of suffering mental and growth delays. During the surgery, doctors will reposition the bulging area back into the skull, remove protrusions, and correct the deformity, thereby relieving pressure that can delay normal brain development. “I would love to have my son treated,” says Jeremy’s mother, “just so that he has an opportunity to live healthily and normally like other children.”

$780raised
Fully funded

“Thank you so much for this support, for keeping my daughter in your heart,” says Ingrid's mother. Ingrid is a 23-month-old girl from Guatemala who is acutely malnourished. “She is much too small for her age since she has not had access to a diverse and caloric diet,” explains our medical partner, Wuqu' Kawoq (WK). “Her diet has not only made her unable to gain weight, but has left her immune system too weak to fight off illnesses such as diarrhea, fevers, and cough--which can be lethal in a child like Ingrid that has a compromised immune system.” WK goes on to say, “Ingrid’s mother is worried because she noticed that she gets sick more often than the other children in the neighborhood.” Indigenous Guatemalans are one of the most marginalized and vulnerable populations in the world. They live in rural areas and suffer from high rates of food insecurity. The poorest indigenous Guatemalan villages have the highest rates of stunting in the world. $512 will fund a multifaceted treatment for Ingrid's malnutrition. WK explains, “This treatment will greatly improve Ingrid's quality of life. She will receive food supplementation, deworming medication, growth monitoring, and micronutrients that will help her grow and develop healthily. Ingrid’s parents will also receive intense nutrition education so they feel empowered to give her the varied diet she needs." Ingrid is the youngest of five children. She loves to play with her older siblings and her older sister's doll. Let's help her get back track so that she can reach a positive growth trajectory.

$512raised
Fully funded

Sarah, a 10-year-old student in Kenya, was out with her mother and two siblings over the holidays and "were involved in a road traffic accident in which two people died," our medical partner, African Mission Healthcare Foundation (AMHF), shares. Immediately after the accident, Sarah and her family were taken to the hospital by good samaritans, and "are lucky to be alive," AMHF says. Sarah's right hand was fractured, and "an X-ray done confirmed the fracture and the surgeon ordered an ORIF (open reduction internal fixation) to be done." Right now, "Sarah is experiencing pain and inability to use the hand." Her mother shares that Sarah "was supposed to report back to school after the holidays but now she can't" because of her injury. Being the oldest of three children, her family has high hopes for Sarah's education. Sarah's father is a casual laborer at the local open air market, and her mother cares for their children. AMHF adds that the family "lives on very little; they live from hand to mouth" and are not in a position to meet the cost of this surgery. $1,125 covers the cost of the treatment that Sarah needs to be able to return to school with a healthy hand. Funds cover the cost of surgery supplies, meals, medicines, and post-operative care. During the procedure, doctors will go in and realign the broken bones and then fix them in place to ensure they heal properly. AMHF shares that Sarah's father was immensely distressed after the accident. "Please help my girl, the others are also here in the ward and I don’t know what to do." Despite the injuries, he still looks towards an optimistic future. "I pray that Watsi will help my daughter so that her hand can be well again to enable her continue with her studies. She is the hope of our family.”

$1,125raised
Fully funded